皮质醇水平与18岁极早产儿童的新生儿疼痛暴露有关 两个独立队列中的月。

Paediatric & neonatal pain Pub Date : 2023-05-29 eCollection Date: 2023-09-01 DOI:10.1002/pne2.12112
Mia A McLean, Lisa Nakajima, Cecil M Y Chau, Joanne Weinberg, Anne R Synnes, Steven P Miller, Ruth E Grunau
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引用次数: 0

摘要

新生儿重症监护室(NICU)频繁的侵入性手术导致的疼痛相关压力与极早产(≤32)儿童的生理压力调节、神经发育和行为改变有关 妊娠周)。此前,在2003-2006年出生的一个队列(队列1)中,我们发现,在18岁时 月校正年龄(CA),出生时胎龄极低的儿童(ELGA;24-28 周)和极低胎龄(VLGA;29-32 周),与足月出生的儿童相比,在涉及认知挑战的发展评估中,测试前皮质醇水平较高,皮质醇输出模式不同(FT;39-41 周)。此外,早产儿中更多的新生儿疼痛相关压力暴露与测试前皮质醇水平较高有关。考虑到早产儿新生儿疼痛的长期不良影响,以及近年来在新生儿重症监护室适当管理疼痛的临床问题的增加,我们旨在检验我们在队列1中的发现是否在2006-2011年出生的独立队列(队列2)中仍然明显,该队列是从加拿大温哥华的同一个三级新生儿重症监护病房招募的。我们还比较了两组患者的皮质醇模式、临床和社会人口学因素及其相互关系。在第2队列中,我们使用多层次建模的研究结果支持并扩展了我们在第1队列中的早期研究结果,表明出生于ELGA的儿童在测试前表现出比FT更高的皮质醇水平。此外,评估中皮质醇输出更大与出生于VLGA的儿童更多的焦虑/抑郁行为有关。重要的是,与第1组相比,第2组中出生的ELGA儿童暴露于更少的新生儿疼痛/压力、机械通气和吗啡。然而,在这两个队列中,皮质醇水平和模式与新生儿疼痛/压力和临床因素(机械通气天数、总体吗啡暴露量)有关。尽管与第1组相比,第2组受疼痛/压力和不良临床因素的影响较小,但在两个独立的队列中,CA 18个月时早产儿的皮质醇水平和认知挑战模式是一致的。这些发现强调,尽管新生儿护理有所改善,但极早产儿童的HPA轴活性仍在改变,这与他们较差的神经发育和行为结果有关。
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Cortisol levels are related to neonatal pain exposure in children born very preterm at age 18 months in two independent cohorts.

Exposure to pain-related stress from frequent invasive procedures in the neonatal intensive care unit (NICU) has been associated with altered physiological stress regulation, neurodevelopment, and behavior in children born very preterm (≤32 weeks gestation). Previously, in a cohort born 2003-2006 (Cohort 1), we found that, at 18 months corrected age (CA), children born extremely low gestational age (ELGA; 24-28 weeks) and very low gestational age (VLGA; 29-32 weeks), had higher pre-test cortisol levels and a different pattern of cortisol output across a developmental assessment involving cognitive challenge compared to children born full-term (FT; 39-41 weeks). Also, greater neonatal pain-related stress exposure among the preterm children was related to higher pre-test cortisol levels. Given the adverse long-term effects of neonatal pain in preterm infants and the ensuing rise in clinical concerns to appropriately manage pain in the NICU in recent years, we aimed to examine whether our findings from Cohort 1 would still be evident in an independent cohort (Cohort 2) born 2006-2011 and recruited from the same tertiary NICU in Vancouver, Canada. We also compared the cortisol patterns, clinical and socio-demographic factors, and their interrelationships between the two cohorts. In Cohort 2, our findings using multi-level modeling support and extend our earlier findings in Cohort 1, demonstrating that children born ELGA display higher pre-test cortisol levels than FT. As well, greater cortisol output across assessment was related to more anxiety/depressive behaviors in children born VLGA. Importantly, children born ELGA were exposed to less neonatal pain/stress, mechanical ventilation, and morphine in Cohort 2 than Cohort 1. In both cohorts, however, cortisol levels and patterns were related to neonatal pain/stress and clinical factors (days on mechanical ventilation, overall morphine exposure). Despite less exposure to pain/stress and adverse clinical factors in Cohort 2 compared to Cohort 1, cortisol levels and patterns across cognitive challenge in preterm children at 18-month CA were consistent across the two independent cohorts. These findings highlight that, despite improvements to neonatal care, children born extremely preterm continue to display altered HPA axis activity, which is associated with their poorer neurodevelopmental and behavioral outcomes.

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Perceived distress due to nasopharyngeal swab collection: Correspondence. Special issue on “Children's and adolescents' rights to participate in their pain management” Pain communication in children with autism spectrum disorder: A scoping review Cortisol levels are related to neonatal pain exposure in children born very preterm at age 18 months in two independent cohorts. Co-occurring chronic pain and primary psychological disorders in adolescents: A scoping review.
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